Sitafloxacin in the treatment of patients with infections caused by vancomycin-resistant enterococci and methicillin-resistant Staphylococcus aureus.

Abstract

Sitafloxacin is a new quinolone active against multi-resistant Gram-positive pathogens. An open study was conducted in patients with serious systemic infections with methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant enterococcus (VRE). Patients with MRSA were recruited if treatment with glycopeptides had failed. Of 11 patients with MRSA infection, four were cured, six failed treatment and one was indeterminate. Of nine patients with VRE infection (one patient had both pathogens), five were cured and four failed. Fifteen adverse events in 12 patients were potentially related to the study drug. Sitafloxacin was effective in VRE and some recalcitrant MRSA infections.

• Authors: N Shetty, A P Wilson
• Journal: The Journal of antimicrobial chemotherapy (J Antimicrob Chemother) Vol. 46 Issue 4 Pg. 633-8 (Oct 2000) ISSN: 0305-7453 [Print] England
• PMID: 11020265 (Publication Type: Clinical Trial, Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Infective Agents
• Fluoroquinolones
• sitafloxacin

Topics

• Adolescent
• Adult
• Aged
• Anti-Infective Agents (pharmacology, therapeutic use)
• Enterococcus (drug effects)
• Fluoroquinolones
• Gram-Positive Bacterial Infections (drug therapy)
• Humans
• Methicillin Resistance (physiology)
• Middle Aged
• Staphylococcal Infections (drug therapy)
• Staphylococcus aureus (drug effects)
• Vancomycin Resistance (physiology)